Abstract

BackgroundCurrently there is no satisfactory explanation for why bacterial insertion sequences (ISs) widely occur across prokaryotes despite being mostly harmful to their host genomes. Rates of horizontal gene transfer are likely to be too low to maintain ISs within a population. IS-induced beneficial mutations may be important for both prevalence of ISs and microbial adaptation to changing environments but may be too rare to sustain IS elements in the long run. Environmental stress can induce elevated rates of IS transposition activities; such episodes are known as ‘transposition bursts’. By examining how selective forces and transposition events interact to influence IS dynamics, this study asks whether transposition bursts can lead to IS persistence.ResultsWe show through a simulation model that ISs are gradually eliminated from a population even if IS transpositions occasionally cause advantageous mutations. With beneficial mutations, transposition bursts create variation in IS copy numbers and improve cell fitness on average. However, these benefits are not usually sufficient to overcome the negative selection against the elements, and transposition bursts amplify the mean fitness effect which, if negative, simply accelerates the extinction of ISs. If down regulation of transposition occurs, IS extinctions are reduced while ISs still generate variation amongst bacterial genomes.ConclusionsTransposition bursts do not help ISs persist in a bacterial population in the long run because most burst-induced mutations are deleterious and therefore not favoured by natural selection. However, bursts do create more genetic variation through which occasional advantageous mutations can help organisms adapt. Regulation of IS transposition bursts and stronger positive selection of the elements interact to slow down the burst-induced extinction of ISs.Electronic supplementary materialThe online version of this article (doi:10.1186/s12862-015-0560-5) contains supplementary material, which is available to authorized users.

Highlights

  • There is no satisfactory explanation for why bacterial insertion sequences (ISs) widely occur across prokaryotes despite being mostly harmful to their host genomes

  • In the third scenario, we introduce a transposition burst at the 5000th generation and allow regulation of the transposition burst to evolve over time

  • In this study we have investigated the role of transposition bursts on the survival of ISs in a bacterial population by modelling the effects of IS movements on the fitness of host genomes

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Summary

Introduction

There is no satisfactory explanation for why bacterial insertion sequences (ISs) widely occur across prokaryotes despite being mostly harmful to their host genomes. Rates of horizontal gene transfer are likely to be too low to maintain ISs within a population. Insertion sequences (ISs) are simple, widely observed mobile genetic elements that only contain genes related to transposition and the regulation of transposition [1,2,3,4,5]. Transposition events can shift, replicate, or delete copies of ISs within a genome, which may induce mutations that change fitness of the host cell [3, 6, 7]. The selfish DNA hypothesis asserts that ISs are able to persist through their ability to self-replicate while making no fitness contribution to the genome [11, 12]. The role of HGT in maintaining ISs within a population is still

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